DRD1, dopamine receptor D1, 1812

N. diseases: 181; N. variants: 8
Disease: Autistic Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.320 Biomarker disease BEFREE This study is to determine the association of single-nucleotide polymorphisms in dopa decarboxylase (DDC) and dopamine receptor-1 (DRD1) genes with childhood autism, in a Chinese Han population. 26337060 2016
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.320 Biomarker disease CTD_human A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families. 18205172 2008
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.320 GeneticVariation disease LHGDN A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families. 18205172 2008